Canonical Allele Identifier: PA916037689
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 613
ClinVar RCV Id: RCV000000644 RCV000089148
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341233.1:p.Phe299Cys
CA251541
NM_001354304.2:c.896T>G